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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148117copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,611,360-89,264,122 , GRCh38.p12 chr10: 79,851,604-87,504,365 ANXA11, FAM245A, 115 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093895copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,428,449-89,725,229 , GRCh38.p12 chr10: 86,668,692-87,965,472 LOC105378410, PAPSS2, 33 more genes
    nsv7074617inversion1nstd229human GRCh38 chr10: 86,025,751-89,446,782 , GRCh37.p13 chr10: 87,785,508-91,206,539 GRID1, LDB3, 83 more genes
    nsv7073898inversion1nstd229human GRCh38 chr10: 85,457,267-89,078,986 , GRCh37.p13 chr10: 87,217,024-90,838,743 LOC112268064, LOC105378416, 74 more genes
    nsv7073504inversion1nstd229human GRCh38 chr10: 87,307,881-87,420,099 , GRCh37.p13 chr10: 89,067,638-89,179,856 NUTM2D, NUTM2A-AS1, 4 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv7061044inversion1nstd229human GRCh38 chr10: 87,238,952-87,520,846 , GRCh37.p13 chr10: 88,998,709-89,280,603 LINC00863, LOC112268064, 8 more genes
    nsv6897572copy number variation1nstd229human GRCh38 chr10: 87,224,501-87,356,900 , GRCh37.p13 chr10: 88,984,258-89,116,657 LINC00863, NUTM2A, 2 more genes
    nsv6897046copy number variation1nstd229human GRCh38 chr10: 87,217,601-87,370,100 , GRCh37.p13 chr10: 88,977,358-89,129,857 NUTM2A, NUTM2A-AS1, 2 more genes
    nsv6896568copy number variation1nstd229human GRCh38 chr10: 87,232,901-87,354,400 , GRCh37.p13 chr10: 88,992,658-89,114,157 LINC00863, NUTM2A, 1 more genes
    nsv6895534copy number variation1nstd229human GRCh38 chr10: 87,223,601-87,356,700 , GRCh37.p13 chr10: 88,983,358-89,116,457 NUTM2D, NUTM2A-AS1, 2 more genes
    nsv6893969copy number variation1nstd229human GRCh38 chr10: 87,153,479-87,410,145 , GRCh37.p13 chr10: 88,913,236-89,169,902 NUTM2A-AS1, NUTM2A, 8 more genes
    nsv6884852copy number variation1nstd229human GRCh38 chr10: 87,223,701-87,368,900 , GRCh37.p13 chr10: 88,983,458-89,128,657 LINC00863, NUTM2A-AS1, 2 more genes
    nsv6880454copy number variation1nstd229human GRCh38 chr10: 87,222,301-87,370,000 , GRCh37.p13 chr10: 88,982,058-89,129,757 NUTM2A-AS1, NUTM2D, 2 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6585055inversion1nstd223human GRCh38 chr10: 79,754,380-87,461,415 , GRCh37.p13 chr10: 81,514,136-89,221,172 DYDC2, LOC105378394, 114 more genes
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